Methocarbamol
- Product NDC
- 60429-118
- 11-digit product format
- 604290118
- Labeler code
- 60429
- Product ID
- 60429-118_d9e4ccc0-0553-2253-e053-2a95a90a2021
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2011-10-21
- Marketing end
- 2024-01-31
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-118-01 | 60429011801 | 100 TABLET, FILM COATED in 1 BOTTLE (60429-118-01) | 2014-02-20 | 0000-00-00 | No | No | Current |
| 60429-118-05 | 60429011805 | 500 TABLET, FILM COATED in 1 BOTTLE (60429-118-05) | 2014-02-20 | 0000-00-00 | No | No | Current |